Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_assertion description "[These findings confirm that mutations in the SCN1A gene are mainly involved in the pathogenesis of SMEI, rarely in that of SIGEI, and are commonly not found in patients with MAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_assertion evidence source_evidence_literature NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_assertion SIO_000772 19464834 NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_assertion wasDerivedFrom befree-20140225 NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_assertion wasGeneratedBy ECO_0000203 NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532602.RAZ2dJHrnQP_9wrmtzZ-Leah_NoM75Yx6tkp3f94hr0vI130_provenance.